skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Process for biological material carbon-carbon bond formation

Patent ·
OSTI ID:872055
 [1];  [2];  [3]
  1. Haslett, MI
  2. Kuyngkido, KR
  3. Lansing, MI
+ Show Author Affiliations

A process for providing vicinal dimethyl long chain between alkyl groups of organic compounds is described. The process uses intact or disrupted cells of various species of bacteria, particularly Thermoanaerobacter sp., Sarcina sp. and Butyrivibrio sp. The process can be conducted in an aqueous reaction mixture at room temperatures.

Research Organization:
Michigan State Univ., East Lansing, MI (United States)
DOE Contract Number:
FG02-89ER14029
Assignee:
Board of Trustees operating Michigan State University (East Lansing, MI)
Patent Number(s):
US 5851807
OSTI ID:
872055
Country of Publication:
United States
Language:
English

References (17)

Membrane lipid alkyl chain motional dynamics is conserved in Sarcina ventriculi despite pH-induced adaptative structural modifications including alkyl chain tail to tail coupling journal September 1995
Böckcr — Books journal September 1974
USE OF GLASS ELECTRODES TO MEASURE ACIDITIES IN DEUTERIUM OXIDE 1,2 journal January 1960
Biology of the sugar-fermenting Sarcinae. journal January 1970
Extrusion of iron-sulfide (Fe2S2* and Fe4S4*) cores from the active sites of ferredoxin proteins journal January 1975
The Effect of the Proton and of Monovalent Cations on Membrane Fluidity book January 1983
Cyclopropanes. XXXVIII. Effect of 1-substituents on the stereochemical stability of the cyclopropyl radical journal March 1976
Synthetic analogs of the active sites of iron-sulfur proteins. VII. Ligand substitution reactions of the tetranuclear clusters [Fe4S4(SR)2- and the structure of bis(tetramethylammonium) [tetra-.mu.-sulfide-tetrakis(benzenethiolato)tetrairon journal June 1974
A new series of long-chain dicarboxylic acids with vicinal dimethyl branching found as major components of the lipids of Butyrivibrio spp journal December 1979
On the Decarbonmonoxylation Reaction journal June 1952
Synthetic analogs of the active sites of iron-sulfur proteins. IX. Formation and some electronic and reactivity properties of iron sulfide (Fe4S4) glycyl-L-cysteinylglycyl oligopeptide complexes obtained by ligand substitution reactions journal September 1974
A mathematical model explaining the molecular weights and distribution of very long chain dicarboxylic acids formed during the adaptive response of sarcina ventriculi journal January 1995
Sarcina ventriculi synthesizes very long chain dicarboxylic acids in response to different forms of environmental stress. journal February 1993
9-Decalyl free radicals. Decomposition of cis- and trans-9-decalylcarbinyl hypochlorite journal April 1967
A new family of very long chain alpha,omega-dicarboxylic acids is a major structural fatty acyl component of the membrane lipids of Thermoanaerobacter ethanolicus 39E. journal June 1994
Structures and stereochemistry of the very long alpha, omega-bifunctional alkyl species in the membrane of Sarcina ventriculi indicate that they are formed by tail-to-tail coupling of normal fatty acids. journal November 1994
Homeoviscous Adaptation--A Homeostatic Process that Regulates the Viscosity of Membrane Lipids in Escherichia coli journal February 1974

Similar Records

Related Subjects

process
biological
material
carbon-carbon
bond
formation
providing
vicinal
dimethyl
chain
alkyl
organic
compounds
described
intact
disrupted
cells
various
species
bacteria
particularly
thermoanaerobacter
sp
sarcina
butyrivibrio
conducted
aqueous
reaction
mixture
temperatures
organic compound
organic compounds
reaction mixture
carbon bond
biological material
aqueous reaction
/435/